A surgical access device includes a seal assembly having a seal housing and a gimbal mount disposed within the seal housing, the seal housing defining a central longitudinal axis and having a longitudinal passage for receiving at least one surgical object therethrough and the gimbal mount adapted for angular movement relative to the central longitudinal axis. The seal assembly also includes a bellows configured to engage at least a portion of the gimbal mount, the bellows dimensioned and adapted to establish a biasing relationship with the gimbal mount, such that the bellows biases the gimbal mount to align with the central longitudinal axis of the seal housing. The bellows is configured to be attached to a proximal wall of the seal housing.
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1. A surgical access device comprising:
a seal assembly including a seal housing and a gimbal assembly disposed within the seal housing, the seal housing defining a central longitudinal axis and having a longitudinal passage for receiving at least one surgical object therethrough, the gimbal assembly adapted for angular movement relative to the central longitudinal axis; and
a bellows extending between the seal housing and the gimbal assembly, the bellows dimensioned and adapted to establish a biasing relationship with the gimbal assembly such that the bellows biases the gimbal assembly to align with the central longitudinal axis of the seal housing, wherein the seal housing includes an extension portion disposed between the bellows and the longitudinal passage and the extension portion is hemispherical.
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This is a continuation of U.S. patent application Ser. No. 14/156,530, filed Jan. 16, 2014, which claims the benefit of and priority to U.S. Provisional Patent Application No. 61/767,358, filed Feb. 21, 2013, the entire disclosure of which is incorporated by reference herein.
The present disclosure relates to a seal system adapted to permit the introduction of surgical instrumentation into a patient's body. In particular, the present disclosure relates to a seal system for use with an introducer or access device, which is intended for insertion into a patient's body, and to receive an instrument in sealing engagement therewith.
Minimally invasive and laparoscopic procedures generally require that any instrumentation inserted into the body is sealed, i.e., provisions must be made to ensure that gases and/or fluids do not enter or exit the body through an endoscopic incision, such as, for example in surgical procedures where the surgical region is insufflated. For such procedures, the introduction of a tube into anatomical cavities, such as the peritoneal cavity, is usually accomplished by use of a system incorporating a trocar and cannula assembly. Since the cannula is in direct communication with the interior of the peritoneal cavity, insertion of the cannula into an opening in the patient's body to reach the inner abdominal cavity should be adapted to maintain a fluid tight interface between the abdominal cavity and the outside atmosphere.
In view of the need to maintain the atmospheric integrity of the inner area of the cavity, a seal assembly for a cannula, which permits introduction of a wide range of surgical instrumentation and maintains the atmospheric integrity of the inner area of the cavity, is desirable. In this regard, there have been a number of attempts in the prior art to achieve such sealing requirements. A difficulty encountered with conventional seal assemblies, however, is the inability of accommodating the wide range of sizes of instrumentation. In addition, angulation and/or manipulation of instrumentation within the cannula often present difficulties with respect to maintaining seal integrity.
According to one aspect of the present disclosure, a surgical access device is provided. The surgical access device includes a seal assembly including a seal housing and a gimbal mount disposed within the seal housing, the seal housing defining a central longitudinal axis and having a longitudinal passage for receiving at least one surgical object therethrough and the gimbal mount adapted for angular movement relative to the central longitudinal axis. The seal assembly also includes a bellows configured to engage at least a portion of the gimbal mount, the bellows dimensioned and adapted to establish a biasing relationship with the gimbal mount, such that the bellows biases the gimbal mount to align with the central longitudinal axis of the seal housing. The bellows is configured to be attached to a proximal wall of the seal housing.
In previous seal arrangements, when a movable valve is in a position in which its longitudinal passage is misaligned with the central longitudinal axis, friction that exists between the valve, e.g., a gimbal mount, and the seal housing causes the longitudinal passage of the valve to be out of alignment with the central longitudinal axis. When this occurs, insertion of instruments through the valve is more likely to tear or otherwise damage the valve, because the sharp tip of such an instrument engages the elastomeric material adjacent to the passage, rather than passing directly through the passage, or else engages the elastomeric material too far from the passage such that the valve is unable to move sufficiently before being torn. By biasing the longitudinal passage of the seal assembly towards the central longitudinal axis, the bellows overcomes the frictional relationship that exists between the gimbal mount and the seal housing, and thereby may decrease the likelihood that the gimbal mount will be damaged during use. In addition, the use of a bellows provides an additional sealing benefit, as insufflation gas is not permitted by the bellows from escaping between the gimbal mount and the seal housing. Attaching the bellows to the proximal wall of the seal housing also decreases or eliminates the need for additional spacing within the seal housing in a location proximal to the gimbal mount, thereby enabling the height of the seal housing to be reduced. Still further, the bellows provides a relatively small amount of biasing force to the gimbal mount—such a small force may be advantageous when a surgeon is using the device. More specifically, the bellows provides for a biasing force that is large enough to enable the benefits of self-centering the gimbal mount, but small enough such that manipulation of an instrument within the seal won't cause the passage of the seal to become “cat-eyed” or stretched to a degree that would cause leakage.
In one exemplary embodiment, the gimbal mount defines a substantially parabolic configuration.
In yet another exemplary embodiment, the seal assembly includes an upper housing portion and a lower housing portion, the upper housing portion mechanically cooperating with the bellows such that the bellows is circumferentially adjacent the longitudinal passage of the seal housing.
In another exemplary embodiment, the upper housing portion defines an angular opening therethrough to facilitate angular reception of the at least one surgical object.
Additionally, the bellows is dimensioned and adapted to inhibit passage of fluids through the seal housing. The bellows may have a uniform wall thickness of about 0.01 inches.
In one exemplary embodiment, the bellows extends to the proximal wall of the seal housing in parallel to the central longitudinal axis defined through the seal housing.
In another exemplary embodiment, the bellows is positioned within a space such that the gimbal mount is movable relative to the seal housing, the space defined between an inner wall and an outer wall of the seal housing.
In yet another exemplary embodiment, one side of the bellows expands and another side of the bellows contracts as the at least one surgical instrument in inserted through and maneuvered within the longitudinal passage of the seal housing.
In an alternative embodiment, the bellows connects to the gimbal mount to form a single integral unit.
In another aspect of the present disclosure, a cannula assembly is provided. The cannula assembly includes a cannula housing, a cannula sleeve extending distally from the cannula housing and a seal assembly disposed in mechanical cooperation with the cannula housing. The seal assembly includes a seal assembly including a seal housing and a gimbal mount disposed within the seal housing, the seal housing defining a central longitudinal axis and having a longitudinal passage for receiving at least one surgical object therethrough and the gimbal mount adapted for angular movement relative to the central longitudinal axis. The seal assembly also includes a bellows configured to engage at least a portion of the gimbal mount, the bellows dimensioned and adapted to establish a biasing relationship with the gimbal mount, such that the bellows biases the gimbal mount to align with the central longitudinal axis of the seal housing. The bellows is configured to be attached to a proximal wall of the seal housing.
Further scope of applicability of the present disclosure will become apparent from the detailed description given hereinafter. However, it should be understood that the detailed description and specific examples, while indicating preferred embodiments of the present disclosure, are given by way of illustration only, since various changes and modifications within the spirit and scope of the present disclosure will become apparent to those skilled in the art from this detailed description.
The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate embodiments of the disclosure and, together with a general description of the disclosure given above, and the detailed description of the embodiment(s) given below, serve to explain the principles of the disclosure, wherein:
The figures depict preferred embodiments of the present disclosure for purposes of illustration only. One skilled in the art will readily recognize from the following discussion that alternative embodiments of the structures and methods illustrated herein may be employed without departing from the principles of the present disclosure described herein.
Particular embodiments of the present disclosure are described hereinbelow with reference to the accompanying drawings. However, it is to be understood that the disclosed embodiments are merely exemplary of the disclosure and may be embodied in various forms. Well-known functions or constructions are not described in detail to avoid obscuring the present disclosure in unnecessary detail. Therefore, specific structural and functional details disclosed herein are not to be interpreted as limiting, but merely as a basis for the claims and as a representative basis for teaching one skilled in the art to variously employ the present disclosure in virtually any appropriately detailed structure.
For the purposes of promoting an understanding of the principles of the present disclosure, reference will now be made to the exemplary embodiments illustrated in the drawings, and specific language will be used to describe the same. It will nevertheless be understood that no limitation of the scope of the present disclosure is thereby intended. Any alterations and further modifications of the inventive features illustrated herein, and any additional applications of the principles of the present disclosure as illustrated herein, which would occur to one skilled in the relevant art and having possession of this disclosure, are to be considered within the scope of the present disclosure.
The seal assembly of the present disclosure, either alone or in combination with a seal system internal to a cannula assembly, provides a substantial seal between a body cavity of a patient and the outside atmosphere before, during and after insertion of an instrument through the cannula assembly. Moreover, the seal assembly of the present disclosure is capable of accommodating instruments of varying diameters, e.g., from 5 mm to 15 mm, by providing a fluid tight seal with each instrument when inserted. The flexibility of the present seal assembly greatly facilitates endoscopic surgery where a variety of instruments having differing diameters are often needed during a single surgical procedure.
The seal assembly contemplates the introduction and manipulation of various types of instrumentation adapted for insertion through a trocar and/or cannula assembly while maintaining a fluid tight interface about the instrumentation to preserve the atmospheric integrity of a surgical procedure from gas and/or fluid leakage. Specifically, the seal assembly accommodates angular manipulation of the surgical instrument relative to the seal housing axis. This feature of the present disclosure desirably minimizes the entry and exit of gases and/or fluids to/from the body cavity. Examples of instrumentation include clip appliers, graspers, dissectors, retractors, staplers, laser probes, photographic devices, endoscopes and laparoscopes, tubes, and the like. Such instruments will be collectively referred to herein as “instruments or instrumentation.”
Embodiments of the presently disclosed apparatus will now be described in detail with reference to the drawings, in which like reference numerals designate identical or corresponding elements in each of the several views. As used herein, the term “distal” refers to that portion of the tool, or component thereof which is further from the user while the term “proximal” refers to that portion of the tool or component thereof which is closer to the user.
Reference will now be made in detail to embodiments of the present disclosure. While certain embodiments of the present disclosure will be described, it will be understood that it is not intended to limit the embodiments of the present disclosure to those described embodiments. To the contrary, reference to embodiments of the present disclosure is intended to cover alternatives, modifications, and equivalents as may be included within the spirit and scope of the embodiments of the present disclosure as defined by the appended claims.
Referring now to the drawings, in which like reference numerals identify identical or substantially similar parts throughout the several views,
Cannula assembly 200 includes cannula sleeve 202 and cannula housing 402 mounted to an end of the sleeve 202. Cannula sleeve 202 defines a longitudinal axis “a” extending along the length of sleeve 202. Sleeve 202 further defines an internal longitudinal passage dimensioned to permit passage of surgical instrumentation. Sleeve 202 may be formed of stainless steel or other rigid materials, such as a polymeric material or the like. Sleeve 202 may be clear or opaque. The diameter of sleeve 202 may vary, but typically ranges from 10 to 15 mm for use with the seal assembly 100 of the present disclosure.
Cannula housing 402 includes two components, specifically, housing flange 206 (see
With reference to
Referring again to
Seal housing 102 incorporates three housing components, namely, proximal, distal and lower housing components 106, 108, 110, respectively, which, when assembled together, form the seal housing 102. The proximal lower housing component 106 may also be referred to as the “upper housing portion,” whereas the distal lower housing components 108, 110 may also be referred to as “lower housing portions.” Assembly of housing components 106, 108, 110 may be affected by any of the aforementioned connection means discussed with respect to cannula housing 402. Therefore, seal housing 102 may be considered as having an upper housing portion formed by component 106, and a detachable lower housing portion formed by components 108, 110.
Proximal housing component 106 defines inner guide wall 112 and outer wall 114 disposed radially outwardly of the inner guide wall 112. Inner guide wall 112 defines central passage 116, which is dimensioned to receive a surgical instrument and laterally confine the instrument within seal housing 102. Inner guide wall 112 is generally cylindrical in configuration and terminates in a distal arcuate surface 118. Outer wall 114 defines an annular recess 120 adjacent its distal end. Recess 120 receives radially spaced tongues (see
Lower housing component 110 is disposed within the interior of distal housing component 108 and is securely connectable to the distal housing component 108 through a bayonet coupling. Such coupling includes radially spaced tongues 124, which depend radially inwardly to be received within correspondingly arranged grooves or recesses 130 on the exterior of lower housing component 110. Coupling of distal and lower housing components 108, 110 is thereby affected through simple rotation of the components.
Seal assembly 100 may be associated with, or joined to, cannula assembly 200 in a variety of ways. In a preferred embodiment, seal housing 102 of seal assembly 100 and cannula housing 402 of cannula assembly 200 are adapted to detachably engage each other, e.g., through a bayonet lock or like mechanical means. As previously discussed, proximal and distal housing components 106, 108 may define an upper housing component 109 (see
With continued reference to
Referring to
The cannula assembly 200 includes an upper cannula housing 402 and a lower cannula housing 404 connected thereto. The lower cannula housing 404 is connected to a cannula sleeve 406 that extends distally from the lower cannula housing 404. The cannula assembly 200 includes an opening 410 at the upper cannula housing 402 for receiving surgical instrumentation therethrough. The cannula sleeve 406 includes an opening 412 at a distal end thereof where the surgical instrumentation exits into, for example, a body cavity of a patient. The lower cannula housing 404 may include a duck bill seal 420 therein, which tapers distally and inwardly to a sealed configuration. Moreover, lower cannula housing 404 may include a luer fitting 416 positioned within a port opening. Luer fitting 416 is adapted for connection to a supply of insufflation gas and incorporates valve 418 to selectively open and close the passage of luer fitting 416.
Referring to
Gimbal mount 504 includes first and second gimbal housings 538, 540 and resilient seal member 542, which is mounted between the housings 538, 540. In a preferred arrangement, first and second gimbal housings 538, 540 and seal member 542 each define a substantially hemispherical configuration. However, one skilled in the art may contemplate a gimbal mount 504 defining a substantially parabolic configuration. First gimbal housing 538 is preferably seated within second gimbal housing 540 and secured to the second gimbal housing 540 through a snap fit connection or the like.
Seal member 542 of gimbal mount 504 is secured in interposed relation between first and second gimbal housings 538, 540. Seal member 542 preferably comprises a resilient center material (e.g., polyisoprene or natural rubber) with first and second layers of fabric 551, 552 impregnated on the respective proximal and distal surfaces of the resilient center material.
Seal member 542 defines central aperture 554 for sealed reception of a surgical instrument (see
Referring to the bellows 510, a second end 513 of bellows 510 is secured in interposed relation between first and second gimbal housings 538, 540. The bellows 510 includes a first end 511 and a second end 513. The bellows 510 is attached or connected to a proximal wall or top wall of the upper cannula housing 402, as will be discussed in detail below. Bellows 510 is shown as a non-linear bellows. However, one skilled in the art may contemplate a plurality of different shapes and sizes for bellows 510. Bellows 510 also includes an opening 553 for receiving surgical instrumentation, as will be discussed in further detail below. Gimbal mount 504 is free to move and is in cooperation with bellows 510 to permit angulation of the instrument relative to the seal axis “c,” while still maintaining a seal thereabout.
Referring to
Referring to both
It is contemplated that the bellows 510 is some type of flexible or semi-rigid rubber structure for re-positioning the gimbal mount 504 in a substantially central position with respect to axis “c,” when the surgical instrument 610 is removed from the opening 553. Bellows 510 may extend around the circumference or periphery of the top portion of the gimbal mount 504.
The gimbal mount 504 and bellows 510 rest within the upper cannula housing 402, such that the first end 511 of the bellows 510 extends toward the proximal end 603 of the upper cannula housing 402, whereas the aperture 554 of the gimbal mount 504 rests on the distal end 601 of the upper cannula housing 402. Additionally, surgical instrument 610 is shown inserted through the opening 553 and a portion of the surgical instrument 610 exiting the aperture 554 to enter into, for example, a body cavity of a patient.
As illustrated, the first end 511 of the bellows 510 is attached or connected to a proximal wall 615 of the upper cannula housing 402. The second end 513 of the bellows 510 seals the radially outer part of the gimbal mount 504 to inhibit leakage, thus eliminating the need for an interface seal or skirt seal, as described above with reference to
In operation, the instrument 610 passes into the lower cannula housing 404 passing through duckbill valve 420 (see
Referring to
Referring to
As shown in
After the surgical instrument 610 has been removed from the cannula assembly 200, bellows 510 enables gimbal mount 504 to move back to its original position (i.e., an unbiased or neutral position). The unbiased position is one where the gimbal mount 504 is centered with respect to axis “c.” Stated differently, bellows 510 may force or propel or guide gimbal mount 504 to return to a position co-axial with the cannula assembly 200. Thus, displacement of gimbal mount 504 from a substantially central position is negated by bellows 510, once the surgical instrument 610 has been removed. Bellows 510 may be moved or adjusted or displaced within the annular space 534 in order to re-position the gimbal mount 504 to a substantially central position with respect to the cannula assembly 200.
Moreover, to reiterate, in
Referring now to
Similarly, second gimbal housing 540 includes a plurality of corresponding locking detents 148 spaced about the interior of the housing 540. Upon insertion of first gimbal housing 538 within second gimbal housing 540, mounting legs 144 slide along locking detents 148 whereby upon clearing the detents 148, locking surfaces 146 of the mounting legs 146 securely engage the locking detents 148 to fix first gimbal housing 538 within second gimbal housing 540 and securing resilient seal member 542 between the components in sandwiched relation. As appreciated, first gimbal housing 538 may be sufficiently resilient to deflect upon insertion to permit mounting legs 144 to clear locking detents 148 and return to their initial position to engage the detents 148.
As mentioned hereinabove, seal member 542 of gimbal mount 504 is secured in interposed relation between first and second gimbal housings 538, 540. Seal member 542 preferably comprises a resilient center material (e.g., polyisoprene or natural rubber) with first and second layers of fabric 550, 552 impregnated on the respective proximal and distal surfaces of the resilient center material. Fabric may be of any suitable fabric for example, a SPANDEX material containing about 20% LYCRA and about 80% NYLON available from Milliken. Seal member 542 defines central aperture 554 for sealed reception of a surgical instrument.
In a preferred arrangement, first layer 550 is arranged to extend or overlap into aperture 554. In this manner, the fabric (which is stronger relative to the resilient material) is positioned to engage the surgical instrument upon passage through aperture 554 of seal member 542 thereby protecting the resilient material defining the aperture. This advantageously minimizes the potential of piercing, penetrating or tearing of the resilient material by the instrument. Alternatively, an additional layer of fabric 551 on the proximal surface of seal member 542 may be superposed and arranged to drape within aperture 554. Seal member 542 includes an annular depression 156 (see
Although seal member 542 is disclosed as an impregnated fabric arrangement, it is appreciated that other seal types may be used and still achieve the objectives of the present disclosure. Further,
With reference now to
Referring to
In operation or use, as the instrument 610 is moved up and down axes “d” or “e,” bellows 510 maintains the instrument 610 in its biased position, as desired by the user. The biased position is an off-center positioned with respect to axis “c,” as illustrated in
Therefore, in summary, with reference to
Referring to
Gimbal mount 2304 includes first and second gimbal housings 2338, 2340 and bellows 2310 has a distal portion which extends between the housings 2338, 2340. In a preferred arrangement, first and second gimbal housings 2338, 2340 each define a substantially hemispherical configuration. However, one skilled in the art may contemplate a gimbal mount 2304 defining a substantially parabolic configuration. First gimbal housing 2338 is preferably seated within second gimbal housing 2340 and secured to the second gimbal housing 2340 through a snap fit connection or the like.
Bellows 2310 defines central aperture 2354 for sealed reception of a surgical instrument. In a preferred arrangement, first layer 2315 is arranged to extend or overlap into aperture 2354. In this manner, the fabric (which is stronger relative to the resilient material) is positioned to engage the surgical instrument upon passage through aperture 2354, thereby protecting the resilient material defining the aperture 2354. Moreover, the distal end 2313 of the bellows 2310 interacts with fabric 2352 to stabilize the distalmost end 2313 to create the aperture 2354. This advantageously minimizes the potential of piercing, penetrating or tearing of the resilient material by the instrument.
Bellows 2310 includes a proximal end 2311 and a distal end 2313. Bellows 2310 extends through the housings 2338, 2340 and up to the aperture 2354. Bellows 2310 also includes an opening 2353 for receiving surgical instrumentation, as will be discussed in further detail below. Gimbal mount 2304 is free to move and is in cooperation with bellows 2310 to permit angulation of the instrument relative to the seal axis “d,” while still maintaining a seal thereabout. Therefore, bellows 2310 is one single integral unit that extends between housing components 2338, 2340 of the gimbal mount 2304.
Referring to
Gimbal mount 2304 is accommodated within an annular space 2334. Gimbal mount 2304 is mounted in a manner that permits angulation of the gimbal mount 2304 relative to seal axis “d.” Specifically, gimbal mount 2304 is free to angulate about an axis or center of rotation “d” through a range of motion defined within the confines of annular space 2334. An annular stop (not shown) may extend within annular space 2334. Annular stop may be positioned to limit the degree of angulation of gimbal mount 2304 if desired. Annular space 2334 includes bellows 2310 for maintaining the gimbal mount 2304 in a biased position when an instrument 2410 is inserted through opening 2353. It is noted that the top portion of the upper cannula housing 2402 include angled portions 2470 for enabling angular insertion of instruments 2410. The angulation allows for easier insertion and manipulation of instruments inserted therethrough.
It is contemplated that the bellows 2310 is some type of flexible or semi-rigid rubber structure for re-positioning the gimbal mount 2304 in a substantially central position with respect to axis “d,” when the surgical instrument 2410 is removed from the opening 2353.
As illustrated, the first end 2311 of the bellows 2310 is attached or connected to a proximal wall 2415 of the upper cannula housing 2402. The second end 2313 of the bellows 2310 seals the radially outer part of the gimbal mount 2304 to inhibit leakage, thus eliminating the need for an interface seal or skirt seal, as described above with reference to
Referring to
As shown in
After the surgical instrument 2410 has been removed from the upper cannula housing 2402, bellows 2310 enables gimbal mount 2304 to move back to its original position (i.e., an unbiased position). The unbiased position is one where the gimbal mount 2304 is centered with respect to axis “d.” Stated differently, bellows 2310 may force or propel or guide gimbal mount 2304 to return to a position co-axial with the upper cannula housing 2402. Thus, displacement of gimbal mount 2304 from a substantially central position is negated by bellows 2310, once the surgical instrument 2410 has been removed. Bellows 2310 may be moved or adjusted or displaced within the annular space 2334 in order to re-position the gimbal mount 2304 to a substantially central position with respect to the upper cannula housing 2402. Moreover, the distal end 2313 of the bellows 2310 is configured to aid the movement of the gimbal mount 2304 since the distal end 2313 of the bellows 2310 is sandwiched between the first and second gimbal housings 2338, 2340, and extends distally up to the central aperture 2354.
Moreover, bellows 2310 is attached or connected or secured to a proximal wall 2415 (or distal end or distal portion/segment or top wall) of the upper cannula housing 2402, thus enabling the bellows 2310 to freely move within the annular space 2334 without any hindrances from any other components. As a result, this configuration seals the radially outward part of the gimbal mount 2304 to the upper cannula housing 2402 to inhibit leakage. Additionally, it also eliminates the need for an interface seal. The vertical structure of the bellows 2310 also provides self-centering that pushes the gimbal mount 2304 toward a center position with respect to axis “d.” Moreover, the width (and overall size of the system) of the upper cannula housing 2402 may be reduced by constructing the bellows 2310 as a vertical structure that connects to the top wall of the upper cannula housing 2402 because less space is required on the sides of the upper cannula housing 2402. Thus, the space between the side walls and the outer surface of the gimbal mount 2304 need not be adapted and dimensioned to accommodate the size of the bellows 2310, as the bellows 2310 extends adjacent the outer surface of the gimbal mount 2304, vertically toward the top wall of the upper cannula housing 2402.
While several embodiments of the disclosure have been shown in the drawings, it is not intended that the disclosure be limited thereto, as it is intended that the disclosure be as broad in scope as the art will allow and that the specification be read likewise. Therefore, the above description should not be construed as limiting, but merely as exemplifications of presently disclosed embodiments. Thus the scope of the embodiments should be determined by the appended claims and their legal equivalents, rather than by the examples given.
Persons skilled in the art will understand that the devices and methods specifically described herein and illustrated in the accompanying drawings are non-limiting exemplary embodiments. The features illustrated or described in connection with one exemplary embodiment may be combined with the features of other embodiments. Such modifications and variations are intended to be included within the scope of the present disclosure. As well, one skilled in the art will appreciate further features and advantages of the present disclosure based on the above-described embodiments. Accordingly, the present disclosure is not to be limited by what has been particularly shown and described, except as indicated by the appended claims.
Patent | Priority | Assignee | Title |
Patent | Priority | Assignee | Title |
5342315, | Apr 12 1993 | EHTICON, INC | Trocar seal/protector assemblies |
5720759, | Jul 14 1993 | United States Surgical Corporation | Seal assembly for accommodating introduction of surgical instruments |
5989224, | Feb 23 1998 | Covidien LP | Universal seal for use with endoscopic cannula |
7582071, | Mar 28 2005 | Covidien LP | Introducer seal assembly |
7632250, | May 10 2002 | Covidien LP | Introducer seal assembly |
7896847, | Mar 28 2005 | Covidien LP | Introducer seal assembly |
7931624, | Apr 05 2005 | Covidien LP | Introducer seal assembly with low profile gimbal seal |
7951118, | May 10 2002 | Covidien LP | Introducer seal assembly |
8357085, | Mar 31 2009 | Cilag GmbH International | Devices and methods for providing access into a body cavity |
9901372, | Feb 21 2013 | Covidien LP | Surgical access device including gimbal mount cooperating with bellows attached to proximal wall of seal housing |
20040066008, | |||
20040068232, | |||
20040204682, | |||
20060224164, | |||
20070088277, | |||
20070255218, | |||
20080125716, | |||
20100049138, | |||
20110124972, | |||
20110196207, | |||
20110201891, | |||
20130310773, | |||
EP638290, | |||
EP2229897, | |||
EP2233090, | |||
GB2287760, | |||
WO3094760, | |||
WO2007121425, | |||
WO9742991, | |||
WO9952577, |
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Jan 09 2018 | United States Surgical Corporation | Covidien LP | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 044940 | /0527 | |
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